ZFIN Human Disease: autosomal dominant intellectual developmental disorder 35

OBO ID: DOID:0070065

Term Name:	autosomal dominant intellectual developmental disorder 35		Search Ontology:
Synonyms:	autosomal dominant mental retardation 35 autosomal dominant non-syndromic intellectual disability 35 MRD35
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the PPP2R5D gene on chromosome 6p21.1. https://www.ncbi.nlm.nih.gov/pubmed/25533962
References:	OMIM:616355
Ontology:	Human Disease ( DOID:0070065 )

Relationships

is a type of:	autosomal dominant intellectual developmental disorder autosomal dominant intellectual developmental disorder Show first 5 Terms

OTHER autosomal dominant intellectual developmental disorder 35 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
PPP2R5D	ppp2r5d	Houge-Janssens syndrome 1	616355

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None